Nature publishes response from Sharpe et al

Competing Financial Interests

M.S. has received royalties from academic writing. T.C. has received royalties from self-help books. J.S. has received royalties from academic writing and payments for acting as an independent medical expert.
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Is this really all they have to declare in this context? This is a genuine question btw, not a rhetorical one. Can we fault them for not mentioning e.g. that M.S. has (according to Coyne) been paid bounties to get people off benefits as an assessor or is this sort of stuff not relevant in this context and/or covered under 'academic writing'?

Even if he may not have to declare this kind of stuff due to hard rules, I somehow feel it gives the proper context to how much he likely actually 'deplores' that people feel 'dismissed by the medical profession'.

Edit: I archived the page as it appears now. This seems pretty serious to me in a broader context. We know that the financial interests these authors have are basically 'their entire careers and also covering our asses from potential lawsuits as soon as anyone notices what we have been doing all this time'. If it is acceptable to Nature that all they declared were some royalties from academic writing and self-help books we would have to re-evaluate everything they publish. I just cannot fathom how the editors could possibly be OK with this.
 
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Snow Leopard said:
What evidence? That CBT/GET don't lead to objective improvements in functioning and no difference in self reports at the long term followup in the PACE trial. Sharpe needs to look at the evidence himself.
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People who are wedded to lies won't accept facts. It would destroy their egos to do so so they must defend their "alternative facts" at any cost :emoji_face_palm:
To them, throwing us under the bus may not be a cost at all, it may be a benefit
 
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Just so people know, there was some discussion of this in the thread about the Nature article.

https://www.s4me.info/threads/natur...igue-syndrome-research.1766/page-3#post-39446

This bit is particularly absurd:

"We think that patients deserve the best research and treatments. In our view, there is no place for stigmatizing any avenue of research or therapy that might help us to improve the lives of people with this long-term debilitating illness."

It's so annoying how they're able to use Cochrane to present themselves as all 'evidence based' while Cochrane ignores all of the problems with their reviews. So much of 'science' seems based more on brand-names than evidence.
 
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